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A Study of LY3437943 in Postmenopausal Female Participants Who Are Overweight or Obese

Overweight Clinical Trial

Official title:
A Phase 1 Study to Investigate the Effect of LY3437943 on the Pharmacokinetics of the Combined Oral Contraceptive Ethinyl Estradiol and Drospirenone in Female Participants

Clinical Trial Summary

The main purpose of this study is to determine the effect of LY3437943 when administered subcutaneously on the levels of combined oral contraceptive (COC) ethinyl estradiol and drospirenone in the blood stream in postmenopausal female participants who are overweight or obese. The safety and tolerability of LY3437943 when administered with COC will also be evaluated. This study will last up to approximately 29 weeks for each participant.

Clinical Trial Description

n/a

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT06039826
Study type Interventional
Source Eli Lilly and Company
Contact
Status Active, not recruiting
Phase Phase 1
Start date September 12, 2023
Completion date July 5, 2024
View Details
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